Cooperation of transmembrane segments during the integration of a double-spanning protein into the ER membrane

被引:85
作者
Heinrich, SU
Rapoport, TA
机构
[1] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
关键词
endoplasmic reticulum membrane; membrane proteins; translocation;
D O I
10.1093/emboj/cdg346
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While membrane insertion of single-spanning membrane proteins into the endoplasmic reticulum (ER) is relatively well understood, it is unclear how multi-spanning proteins integrate. We have investigated the cotranslational ER integration of a double-spanning protein that is derived from leader peptidase. Both transmembrane (TM) segments are inserted into the membrane by the Sec61 channel. While the first, long and hydrophobic TM segment (TM1) inserts into the lipid bilayer on its own, the second, shorter TM anchor (TM2) collaborates with TM1 during its integration. TM1 diffuses away from the Sec61 complex in the absence of TM2, but is close to Sec61 when TM2 arrives inside the channel. These data suggest that the exit of a weak TM segment from the Sec61 channel into the lipid phase can be facilitated by its interaction with a previously integrated strong and stabilizing TM anchor.
引用
收藏
页码:3654 / 3663
页数:10
相关论文
共 25 条
[1]   Architecture of the protein-conducting channel associated with the translating 80S ribosome [J].
Beckmann, R ;
Spahn, CMT ;
Eswar, N ;
Helmers, J ;
Penczek, PA ;
Sali, A ;
Frank, J ;
Blobel, G .
CELL, 2001, 107 (03) :361-372
[2]   INTRACELLULAR PROTEIN TOPOGENESIS [J].
BLOBEL, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (03) :1496-1500
[3]   CONTROLLED PROTEOLYSIS OF NASCENT POLYPEPTIDES IN RAT LIVER CELL FRACTIONS .1. LOCATION OF POLYPEPTIDES WITHIN RIBOSOMES [J].
BLOBEL, G ;
SABATINI, DD .
JOURNAL OF CELL BIOLOGY, 1970, 45 (01) :130-&
[4]   Biogenesis of polytopic membrane proteins: Membrane segments assemble within translocation channels prior to membrane integration [J].
Borel, AC ;
Simon, SM .
CELL, 1996, 85 (03) :379-389
[5]   TOPOLOGICAL FRUSTRATION IN MULTISPANNING ESCHERICHIA-COLI INNER MEMBRANE-PROTEINS [J].
GAFVELIN, G ;
VONHEIJNE, G .
CELL, 1994, 77 (03) :401-412
[6]   Topological rules for membrane protein assembly in eukaryotic cells [J].
Gafvelin, G ;
Sakaguchi, M ;
Andersson, H ;
vonHeijne, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (10) :6119-6127
[7]   Membrane protein biogenesis: Regulated complexity at the endoplasmic reticulum [J].
Hegde, RS ;
Lingappa, VR .
CELL, 1997, 91 (05) :575-582
[8]   The Sec61p complex mediates the integration of a membrane protein by allowing lipid partitioning of the transmembrane domain [J].
Heinrich, SU ;
Mothes, W ;
Brunner, J ;
Rapoport, TA .
CELL, 2000, 102 (02) :233-244
[9]   SEC61P IS ADJACENT TO NASCENT TYPE-I AND TYPE-II SIGNAL-ANCHOR PROTEINS DURING THEIR MEMBRANE INSERTION [J].
HIGH, S ;
ANDERSEN, SSL ;
GORLICH, D ;
HARTMANN, E ;
PREHN, S ;
RAPOPORT, TA ;
DOBBERSTEIN, B .
JOURNAL OF CELL BIOLOGY, 1993, 121 (04) :743-750
[10]   Membrane topogenesis of a type I signal-anchor protein, mouse synaptotagmin II, on the endoplasmic reticulum [J].
Kida, Y ;
Sakaguchi, M ;
Fukuda, M ;
Mikoshiba, K ;
Mihara, K .
JOURNAL OF CELL BIOLOGY, 2000, 150 (04) :719-729